Regulatory Affairs Associate - San Diego

We are seeking a Regulatory Affairs Associate to support U.S. and global regulatory submissions for medical device products. · Bachelor's Degree required, preferably in pharmacy, biology, chemistry, pharmacology, engineering or related subject. · 2–4 years of Regulatory Affairs e ...

We are seeking a Regulatory Affairs Associate II with hands-on medical device regulatory experience to support U.S. and global submissions. · Prepare and manage U.S. and global regulatory submissions (FDA, EU MDR) · Support change assessments and regulatory impact analyses ...

This is an exciting opportunity to join our team as a Regulatory Affairs Associate II in San Diego, CA. As a key member of our team, you will be responsible for preparing regulatory submissions and obtaining approvals. · ...

Regulatory Affairs Associate II role requires a strong understanding of FDA and EU regulations, with experience in preparing regulatory submissions and obtaining approvals. · ...

Direct medical device regulatory experience with recent hands-on EU MDR 2017/745 experience and ISO 13485 familiarity. · Bachelor's Degree in pharmacy, biology, chemistry, pharmacology or related subject. · RAC Certification preferred. · ...

This role supports execution of global regulatory strategies and preparation and maintenance of registration dossiers for U.S. and global medical device submissions. · ...

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The job is for a Regulatory Affairs Associate who will provide regulatory support and expertise associated with US and global submission requirements. The associate will analyze requirements, track deliverables, and execute global regulatory strategies. · ...

Provide regulatory support and expertise associated with US and global submission requirements including analysis of the requirements and tracking of deliverables. Assures full regulatory compliance of all documentation for submissions and change management to enable product appr ...

Provide regulatory support and expertise associated with US and global submission requirements. · ...

The Associate Regulatory Affairs Manager will support the development, review, · and submission of regulatory documents for medical device and IVD products. · This role will assist in managing regulatory projects, · ensuring compliance with FDA, ISO 13485, · and other global regu ...

The Associate Director of Regulatory Affairs is responsible for development and implementation of regulatory affairs strategy as a member of multi-disciplinary pharmaceutical product development teams. · ...

The Associate Director of Regulatory Affairs is responsible for developing and implementing regulatory affairs strategy as a member of multi-disciplinary pharmaceutical product development teams. · Represent Regulatory Affairs in assigned project meetings and provide regulatory g ...

Provide Regulatory CMC support for biologic and small molecule drugs being evaluated or marketed for the treatment of oncology, HIV and liver disease. · ...

The Associate Director of Regulatory Affairs is responsible for development and implementation of regulatory affairs strategy as a member of multi-disciplinary pharmaceutical product development teams. · Represent Regulatory Affairs in assigned project meetings and provide regula ...

+Job summary · The Associate Director of Regulatory Affairs is responsible for development and implementation of regulatory affairs strategy as a member of multi-disciplinary pharmaceutical product development teams. · +QualificationsBachelor's degree required, with an advanced s ...

The Associate Director of Community Affairs is a key member of the Development team and is responsible for strengthening the organization's presence, reputation, · and partnerships within the community.This role develops and manages programming and opportunities for engagement wi ...

+Provide regulatory support and expertise associated with US and global submission requirements. · +Assures full regulatory compliance of all documentation for submissions and change management to enable product approval and issuance of EC certificates, FDA or other international ...

We provide regulatory support and expertise associated with US and global submission requirements. · ...

This role provides regulatory support and expertise associated with US and global submission requirements. · ...